Interventional study of three methods of caring for the donor area of burn trauma patients with skin implants

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2300072772

Enrollment

Unknown

Registered

2023-06-25

Start date

2023-07-01

Completion date

Unknown

Last updated

2023-06-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Burn Trauma

Interventions

Control group:Vaseline oil yarn + infrared baking lamp

Experimental group 1:Sanyrene

Experimental group 2:Sanyrene+ infrared baking lamp

Eligibility

Sex/Gender

All

Age

18 Years to 100 Years

Inclusion criteria

Inclusion criteria: ? Age = 18 years ? Patient informed consent ? Patients with donor area for all types of implant surgery ? Able to communicate accurately verbally and express feelings ? Donor area = 50cm2

Exclusion criteria

Exclusion criteria: ?Patients who are allergic to Cytoxan or Vaseline ?Patients who do not cooperate with intervention and observation ?Patients with psychological or psychiatric problems ?Patients after second or multiple implants ?Patients with combined malignant tumors ?Patients with head donor area ?Patients with combined skin diseases.

Design outcomes

Primary

Measure	Time frame
Wound healing rate;	—

Secondary

Measure	Time frame
Healing time of the donor site wound;Pain score;	—

Countries

CHINA

Contacts

Public ContactQixia Jiang

Eastern War Zone General Hospital

jiangqixia1963@163.com+86 139 5198 7603

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026